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Ultrastructure of the lung in a murine model of malaria-associated acute lung injury/acute respiratory distress syndrome

BACKGROUND: The mechanisms through which infection with Plasmodium spp. result in lung disease are largely unknown. Recently a number of mouse models have been developed to research malaria-associated lung injury but no detailed ultrastructure studies of the disease in its terminal stages in a murin...

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Autores principales: Aitken, Elizabeth H, Negri, Elnara M, Barboza, Renato, Lima, Maria RI, Álvarez, José M, Marinho, Claudio RF, Caldini, Elia G, Epiphanio, Sabrina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4062769/
https://www.ncbi.nlm.nih.gov/pubmed/24927627
http://dx.doi.org/10.1186/1475-2875-13-230
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author Aitken, Elizabeth H
Negri, Elnara M
Barboza, Renato
Lima, Maria RI
Álvarez, José M
Marinho, Claudio RF
Caldini, Elia G
Epiphanio, Sabrina
author_facet Aitken, Elizabeth H
Negri, Elnara M
Barboza, Renato
Lima, Maria RI
Álvarez, José M
Marinho, Claudio RF
Caldini, Elia G
Epiphanio, Sabrina
author_sort Aitken, Elizabeth H
collection PubMed
description BACKGROUND: The mechanisms through which infection with Plasmodium spp. result in lung disease are largely unknown. Recently a number of mouse models have been developed to research malaria-associated lung injury but no detailed ultrastructure studies of the disease in its terminal stages in a murine model have yet been published. The goal was to perform an ultrastructural analysis of the lungs of mice that died with malaria-associated acute lung injury/acute respiratory distress syndrome to better determine the relevancy of the murine models and investigate the mechanism of disease. METHODS: DBA/2 mice were infected with Plasmodium berghei strain ANKA. Mice had their lungs removed immediately after death, processed using standard methods and viewed by transmission electron microscopy (TEM). RESULTS: Infected red blood cell:endothelium contact, swollen endothelium with distended cytoplasmic extensions and thickening of endothelium basement membrane were observed. Septa were thick and filled with congested capillaries and leukocytes and the alveolar spaces contained blood cells, oedema and cell debris. CONCLUSION: Results show that the lung ultrastructure of P. berghei ANKA-infected mice has similar features to what has been described in post-mortem TEM studies of lungs from individuals infected with Plasmodium falciparum. These data support the use of murine models to study malaria-associated acute lung injury.
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spelling pubmed-40627692014-06-20 Ultrastructure of the lung in a murine model of malaria-associated acute lung injury/acute respiratory distress syndrome Aitken, Elizabeth H Negri, Elnara M Barboza, Renato Lima, Maria RI Álvarez, José M Marinho, Claudio RF Caldini, Elia G Epiphanio, Sabrina Malar J Research BACKGROUND: The mechanisms through which infection with Plasmodium spp. result in lung disease are largely unknown. Recently a number of mouse models have been developed to research malaria-associated lung injury but no detailed ultrastructure studies of the disease in its terminal stages in a murine model have yet been published. The goal was to perform an ultrastructural analysis of the lungs of mice that died with malaria-associated acute lung injury/acute respiratory distress syndrome to better determine the relevancy of the murine models and investigate the mechanism of disease. METHODS: DBA/2 mice were infected with Plasmodium berghei strain ANKA. Mice had their lungs removed immediately after death, processed using standard methods and viewed by transmission electron microscopy (TEM). RESULTS: Infected red blood cell:endothelium contact, swollen endothelium with distended cytoplasmic extensions and thickening of endothelium basement membrane were observed. Septa were thick and filled with congested capillaries and leukocytes and the alveolar spaces contained blood cells, oedema and cell debris. CONCLUSION: Results show that the lung ultrastructure of P. berghei ANKA-infected mice has similar features to what has been described in post-mortem TEM studies of lungs from individuals infected with Plasmodium falciparum. These data support the use of murine models to study malaria-associated acute lung injury. BioMed Central 2014-06-13 /pmc/articles/PMC4062769/ /pubmed/24927627 http://dx.doi.org/10.1186/1475-2875-13-230 Text en Copyright © 2014 Aitken et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Aitken, Elizabeth H
Negri, Elnara M
Barboza, Renato
Lima, Maria RI
Álvarez, José M
Marinho, Claudio RF
Caldini, Elia G
Epiphanio, Sabrina
Ultrastructure of the lung in a murine model of malaria-associated acute lung injury/acute respiratory distress syndrome
title Ultrastructure of the lung in a murine model of malaria-associated acute lung injury/acute respiratory distress syndrome
title_full Ultrastructure of the lung in a murine model of malaria-associated acute lung injury/acute respiratory distress syndrome
title_fullStr Ultrastructure of the lung in a murine model of malaria-associated acute lung injury/acute respiratory distress syndrome
title_full_unstemmed Ultrastructure of the lung in a murine model of malaria-associated acute lung injury/acute respiratory distress syndrome
title_short Ultrastructure of the lung in a murine model of malaria-associated acute lung injury/acute respiratory distress syndrome
title_sort ultrastructure of the lung in a murine model of malaria-associated acute lung injury/acute respiratory distress syndrome
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4062769/
https://www.ncbi.nlm.nih.gov/pubmed/24927627
http://dx.doi.org/10.1186/1475-2875-13-230
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